A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948206



Internal ID18595052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:120347273..120355231hg38UCSC Ensembl
Innerchr10:122106785..122114743hg19UCSC Ensembl
Innerchr10:122096775..122104733hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg387959
hg197959
hg187959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1868933, nssv1868935, nssv1868937, nssv1868940, nssv1868938, nssv1868939, nssv1868934, nssv1868932, nssv1868941, nssv1868936
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948206
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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